Kammoun M - Search Results

1

Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss.

Zidi-Jrah I, Hajlaoui A, Mougou-Zerelli S, Kammoun M, Meniaoui I, Sallem A, Brahem S, Fekih M, Bibi M, Saad A, Ibala-Romdhane S. Zidi-Jrah I, et al. Among authors: kammoun m. Fertil Steril. 2016 Jan;105(1):58-64. doi: 10.1016/j.fertnstert.2015.09.041. Epub 2015 Oct 19. Fertil Steril. 2016. PMID: 26493117 Free article.

2

Detection of aneuploidy rate for chromosomes X, Y and 8 by fluorescence in-situ hybridization in spermatozoa from patients with severe non-obstructive oligozoospermia.

Mougou-Zerelli S, Brahem S, Kammoun M, Jerbi M, Elghezal H, Ajina M, Saad A. Mougou-Zerelli S, et al. Among authors: kammoun m. J Assist Reprod Genet. 2011 Sep;28(10):971-7. doi: 10.1007/s10815-011-9621-x. Epub 2011 Aug 19. J Assist Reprod Genet. 2011. PMID: 21853383 Free PMC article.

3

NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.

Bouali N, Francou B, Bouligand J, Lakhal B, Malek I, Kammoun M, Warszawski J, Mougou S, Saad A, Guiochon-Mantel A. Bouali N, et al. Among authors: kammoun m. Clin Genet. 2016 May;89(5):608-13. doi: 10.1111/cge.12750. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26848058

4

Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea.

Ben Hadj Hmida I, Mougou-Zerelli S, Hadded A, Dimassi S, Kammoun M, Bignon-Topalovic J, Bibi M, Saad A, Bashamboo A, McElreavey K. Ben Hadj Hmida I, et al. Among authors: kammoun m. Fertil Steril. 2016 Jul;106(1):225-229.e11. doi: 10.1016/j.fertnstert.2016.03.008. Epub 2016 Mar 22. Fertil Steril. 2016. PMID: 27016457 Free article.

5

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

Khelifa HB, Kammoun M, Hannachi H, Soyah N, Hammami S, Elghezal H, Sanlaville D, Saad A, Mougou-Zerelli S. Khelifa HB, et al. Among authors: kammoun m. J Pediatr Genet. 2015 Dec;4(4):187-93. doi: 10.1055/s-0035-1565269. Epub 2015 Oct 14. J Pediatr Genet. 2015. PMID: 27617130 Free PMC article.

6

Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Kammoun M, Slimani W, Hannachi H, Bibi M, Saad A, Mougou-Zerelli S. Kammoun M, et al. J Pediatr Genet. 2017 Dec;6(4):215-221. doi: 10.1055/s-0037-1602696. Epub 2017 Apr 26. J Pediatr Genet. 2017. PMID: 29142763 Free PMC article.

7

Sperm fluorescent in situ hybridisation study of interchromosomal effect in six Tunisian carriers of reciprocal and Robertsonian translocations.

Hajlaoui A, Slimani W, Kammoun M, Sallem A, Braham S, Bibi M, Saad A, Mougou-Zerelli S. Hajlaoui A, et al. Among authors: kammoun m. Andrologia. 2018 Jan 15. doi: 10.1111/and.12949. Online ahead of print. Andrologia. 2018. PMID: 29336050

8

Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.

Hajlaoui A, Slimani W, Kammoun M, Sallem A, El Amri F, Chaieb A, Bibi M, Saad A, Mougou-Zerelli S. Hajlaoui A, et al. Among authors: kammoun m. Int J Fertil Steril. 2018 Jun;12(3):218-222. doi: 10.22074/ijfs.2018.5260. Epub 2018 Jun 20. Int J Fertil Steril. 2018. PMID: 29935067 Free PMC article.

9

Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization.

Slimani W, Ben Khelifa H, Dimassi S, Chioukh FZ, Jelloul A, Kammoun M, Hannachi H, Bouslah S, Jammali N, Sanlaville D, Saad A, Mougou-Zerelli S. Slimani W, et al. Among authors: kammoun m. Mol Cytogenet. 2019 Feb 8;12:5. doi: 10.1186/s13039-019-0414-8. eCollection 2019. Mol Cytogenet. 2019. PMID: 30774715 Free PMC article.

10

Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case.

Rjiba K, Soyah N, Kammoun M, Hadj Hmida I, Saad A, Mcelreavey K, Mougou-Zerelli S. Rjiba K, et al. Among authors: kammoun m. Eur J Med Genet. 2021 Sep;64(9):104285. doi: 10.1016/j.ejmg.2021.104285. Epub 2021 Jul 3. Eur J Med Genet. 2021. PMID: 34229114

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